2015
DOI: 10.1016/bs.vh.2014.11.002
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Orphanin FQ-ORL-1 Regulation of Reproduction and Reproductive Behavior in the Female

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Cited by 7 publications
(7 citation statements)
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References 169 publications
(279 reference statements)
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“…However, recent investigations in the spinal cord trigeminal neurons and hypothalamus (a unique brain region, which regulates the synthesis of sex steroids) suggest that the progesterone to estrogen ratio, which fluctuates during the menstrual cycle influences NOP receptor expression and binding. These studies have reported increases in NOP in the hypothalamic nuclei following both estrogen and estrogen + progesterone treatment; and decreases in NOP in the trigeminal neurons during the proestrous (high estrogen/low progesterone) compared to diestrous (low estrogen/high progesterone) phase of the rodent menstrual cycle (57,58). It is unclear as to whether, and how menstrual cycle phase may have influenced [ 11 C]NOP-1A V T measurements in the midbrain and cerebellum in this imaging study.…”
Section: Discussionmentioning
confidence: 99%
“…However, recent investigations in the spinal cord trigeminal neurons and hypothalamus (a unique brain region, which regulates the synthesis of sex steroids) suggest that the progesterone to estrogen ratio, which fluctuates during the menstrual cycle influences NOP receptor expression and binding. These studies have reported increases in NOP in the hypothalamic nuclei following both estrogen and estrogen + progesterone treatment; and decreases in NOP in the trigeminal neurons during the proestrous (high estrogen/low progesterone) compared to diestrous (low estrogen/high progesterone) phase of the rodent menstrual cycle (57,58). It is unclear as to whether, and how menstrual cycle phase may have influenced [ 11 C]NOP-1A V T measurements in the midbrain and cerebellum in this imaging study.…”
Section: Discussionmentioning
confidence: 99%
“…What this theory hypothesis does not explain is how estrogens alone induce lordosis, which required higher estrogen doses and a longer interval between estrogen treatment and the behavior (Pfaff, 1970 reviewed in Clemens and Weaver, 1985). What has emerged is the idea that different behavioral circuits are activated by estradiol only treatment compared with estrogen and progesterone (reviewed in Sinchak et al, 2015). In the ARH, estradiol-only facilitation of lordosis reflex requires the activation of the opioid receptor, ORL-1, but estradiol + progesterone does not (Borgquist et al, 2014).…”
Section: Steroid Activation Of Sexual Receptivitymentioning
confidence: 99%
“…Throughout the estrous cycle, the pattern of MPN MOR activation/internalization tracks the sexual receptivity of the female, that is, MOR are deactivated (internalized) on the evening of proestrus when the rat is sexually receptive and reactivated on the morning of estrus when she is no longer receptive (Sinchak and Micevych, 2003; reviewed in Micevych and Sinchak, 2013; Sinchak et al, 2015). …”
Section: Steroid Activation Of Sexual Receptivitymentioning
confidence: 99%
“…Thus far, all steroid paradigms studied regulate the output of ARH β-end neurons in a manner that is congruent with the rat’s sexual behavioral state [9, 47, 48, 59, 60, 84, 90, 93, 101105]. Importantly, the association of behavior and MPN MOR activity is observed in intact cycling rats [95].…”
Section: Membrane Estrogen Receptors Regulating Sexual Receptivitymentioning
confidence: 99%